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Quality Control Laboratory Manager Jobs in Randolph, MA

Replimune

Scientist I, Quality Control

Framingham, MA · On-site

$112K - $146K/yr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Replimune-2

Scientist I, Quality Control

Framingham, MA · On-site

$112.50 - $146/hr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Replimune Group

Scientist I, Quality Control

Framingham, MA · On-site

$112.50 - $146/hr

The QC Analytical Scientist will assist in the management of the QC laboratory. It is expected that the QC Scientist will maintain GMP compliance in the QC laboratory. This position is based in our ...

Rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

rentschler

Quality Control Data Reviewer

Milford, MA · On-site

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.

Rentschler

Quality Control Data Reviewer

Milford, MA · Hybrid

$90K - $110K/yr

Assists in training of new hires and retraining of QC laboratory staff, as needed * Assist/mentor Q ... Provide timely status updates to Management upon request * Proficient with MS Outlook, Word, Excel ...

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All JobsQuality Control Laboratory JobsQuality Control Laboratory Manager JobsQuality Control Laboratory Manager Jobs in Randolph, MA

Quality Control Laboratory Manager information

See Randolph, MA salary details

$31.1K

$82.9K

$132K

How much do quality control laboratory manager jobs pay per year?

As of Aug 30, 2026, the average yearly pay for quality control laboratory manager in Randolph, MA is $82,923.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,700.00 and $102,000.00 per year, depending on experience, location, and employer.

What does a quality control laboratory manager do?

A Quality Control Laboratory Manager oversees the operations of a laboratory that tests products for quality and compliance with industry standards. They manage laboratory staff, ensure testing procedures are followed accurately, and maintain equipment. The manager is responsible for implementing quality assurance protocols, analyzing test results, and reporting findings to upper management. Their work helps ensure that products meet safety and quality requirements before reaching consumers.

What are the key skills and qualifications needed to thrive as a quality control laboratory manager?

To thrive as a Quality Control Laboratory Manager, you need a strong background in laboratory science, quality assurance, and regulatory compliance, typically supported by a relevant degree and industry experience. Familiarity with laboratory information management systems (LIMS), Good Laboratory Practice (GLP), and certifications such as ASQ Certified Quality Auditor are often required. Excellent leadership, problem-solving, and communication skills help manage teams and ensure smooth operations. These competencies are crucial for maintaining high standards, ensuring product safety, and meeting regulatory requirements in laboratory environments.

What are some common challenges faced by quality control laboratory managers, and how can they be addressed?

Quality Control Laboratory Managers often face challenges such as maintaining compliance with strict regulatory standards, managing a diverse team, and ensuring timely turnaround of test results. To address these, effective managers implement robust training programs, foster clear communication across teams, and establish standardized operating procedures. Proactive planning and continuous process improvement are key to staying ahead of regulatory updates and ensuring consistent data quality, which ultimately supports both operational efficiency and product safety.

What is the difference between Quality Control Laboratory Manager vs Quality Control Analyst?

AspectQuality Control Laboratory ManagerQuality Control Analyst
CredentialsBachelor's degree in science, often with management certificationsBachelor's degree in science or related field
Work EnvironmentSupervises lab staff, manages operations, oversees testing processesPerforms testing and analysis of samples under supervision
Employer & Industry UsageUsed in pharmaceutical, biotech, and manufacturing industries for lab oversightCommonly employed in similar industries for sample analysis

The main difference is that the Quality Control Laboratory Manager oversees the entire lab operations and staff, ensuring compliance and quality standards, while the Quality Control Analyst focuses on conducting specific tests and analyses. The manager has more responsibilities related to supervision and process management, whereas the analyst is primarily involved in testing tasks.

What cities near Randolph, MA are hiring for Quality Control Laboratory Manager jobs?

Cities near Randolph, MA with the most Quality Control Laboratory Manager job openings:

Quality Control Laboratory Manager jobs near you
Infographic showing various Quality Control Laboratory Manager job openings in Randolph, MA as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 21% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 3% Hybrid, and 9% Remote job distribution, with an average salary of $82,923 per year, or $39.9 per hour.

Senior Director, QC Laboratory

Candel Therapeutics, Inc.

Needham, MA • On-site

$258 - $285/hr

Other

This job post has expired 2 days ago. Applications are no longer accepted.

Job description

This is a hybrid role in Needham, MA office (2-3 days a week)

Salary: $258,000-$285,000

Why WorkWithUs?

At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission driven environment. Like a team, we show up for each other and stay focused on making a difference for patients and families. Our leadership is transparent and empowering, and our culture is built on trust, flexibility, and accountability, encouraging ownership and innovation every day. If you thrive in a lean, fast moving environment where your work truly matters, you will feel at home here.

Our Science: Advancing Cancer Immunotherapies

Candel is a clinical stage biopharmaceutical company developing off-the-shelf, multimodal cancer immunotherapies designed to stimulate personalized, systemic anti tumor immune responses. Our proprietary platforms leverage genetically modified adenovirus and HSV constructs. With positive Phase 3 results for our lead candidate, this is a pivotal and exciting time to join Candel and help bring transformative cancer treatments to patients.

Position Summary

The Senior Director, QC Laboratory is responsible for the establishment, leadership, and ongoing operation of Candel Therapeutics’ internal GMP Quality Control laboratory.

The Senior Director, QC Laboratory will provide leadership, direction, and technical oversight to the QC team while ensuring compliance with GMP requirements and internal quality standards. This role partners closely with Quality Assurance, Analytical Development, R&D, Manufacturing, and other internal stakeholders to support clinical development activities and future organizational growth.

Essential Areas of Responsibility
  • Provide leadership and oversight for the internal GMP QC laboratory, including establishment of laboratory operations, workflows, and execution standards.
  • Lead, mentor, and develop QC laboratory staff, fostering a collaborative, accountable, and compliant team culture.
  • Directly manage internal QC staff and future laboratory growth, supporting performance, development, and organizational readiness.
  • Ensure QC laboratory operations are conducted in compliance with GMP requirements, internal SOPs, and data integrity expectations.
  • Serve as a key QC partner to Quality Assurance for deviations, investigations, change controls, CAPAs, and inspection readiness activities.
  • Provide hands‑on leadership and operational support in the laboratory environment as needed to meet business and quality objectives.
  • Collaborate cross‑functionally with Analytical Development, R&D, Manufacturing, Regulatory Affairs, and other internal stakeholders to support testing needs and program timelines.
  • Support audit and inspection activities related to QC laboratory operations, documentation, and systems.
  • Implement and maintain practical, scalable QC processes appropriate for a growing biotech organization.
  • Drive continuous improvement initiatives within the QC laboratory while maintaining appropriate controls and compliance.
  • Contribute to staffing plans, onboarding, training, succession planning, and long‑term QC capability development.
Minimum Education, Experience and Skill RequirementsEducation
  • Bachelor’s degree in a scientific discipline required; advanced degree preferred.
Experience
  • Minimum of 10 years of experience in a GMP Quality Control laboratory environment within biotech or pharmaceutical organizations.
  • Demonstrated experience operating within a true QC organization, with a strong understanding of QC structure, controls, and GMP rigor.
  • Prior experience leading, mentoring, or managing QC laboratory staff.
  • Experience supporting GMP inspections, audits, and quality system activities impacting QC operations.
  • Strong interpersonal, leadership, and communication skills with the ability to partner effectively across functions.
  • Comfort working in a build‑phase or evolving environment where systems and infrastructure are developing.
  • Proficiency with standard office software including Microsoft Word, Excel, and PowerPoint.

Must be authorized to work in US. We cannot provide sponsorships.

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